Citregen Tendon Sizing Kit 40-811-0001

GUDID 00810027270283

Acuitive Technologies, Inc.

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• Primary Device ID: 00810027270283
• NIH Device Record Key: 8712189d-29ae-4c88-8240-7acc095d8728
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Citregen Tendon Sizing Kit
• Version Model Number: 40-811-0001
• Catalog Number: 40-811-0001
• Company DUNS: 074645634
• Company Name: Acuitive Technologies, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx
• Phone: 201-661-2680
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810027270283 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200725

FDA Product Code

• HWQ: Passer

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-02
• Device Publish Date: 2020-11-24

Devices Manufactured by Acuitive Technologies, Inc.

• 00810027271471 - Citrelock ACL 1.1mm K-Wire: 2024-03-07
• 00810027270436 - Citrefix 2.9mm Inserter: 2023-07-03
• 00810027270443 - Citrefix 3.5mm Inserter: 2023-07-03
• 00810027270450 - Citrefix 4.5mm Inserter: 2023-07-03
• 00810027270467 - Citrefix 5.5mm Inserter: 2023-07-03
• 00810027270474 - Citrefix 2.9mm Drill: 2023-07-03
• 00810027270481 - Citrefix 3.5mm Drill: 2023-07-03
• 00810027270498 - Citrefix 4.5mm Drill: 2023-07-03